Suppr超能文献

超高效液相色谱-电喷雾电离串联质谱法同时测定水产品中孔雀石绿、结晶紫、亚甲基蓝及其代谢物残留量

Simultaneous determination of malachite green, crystal violet, methylene blue and the metabolite residues in aquatic products by ultra-performance liquid chromatography with electrospray ionization tandem mass spectrometry.

作者信息

Xu Ying-Jiang, Tian Xiu-Hui, Zhang Xiu-Zhen, Gong Xiang-Hong, Liu Hui-Hui, Zhang Huan-Jun, Huang Hui, Zhang Li-Min

机构信息

1Marine Fisheries Research Institute of Shandong Province, Yantai 264006, People's Republic of China.

出版信息

J Chromatogr Sci. 2012 Aug;50(7):591-7. doi: 10.1093/chromsci/bms054. Epub 2012 Apr 26.

Abstract

This work describes solid-phase extraction-ultra-performance liquid chromatography with electrospray ionization tandem spectrometry for determination of malachite green and metabolite leucomalachite green, crystal violet and metabolite leucocrystal violet, methylene blue and metabolites including azure A, azure B and azure C in aquatic products. Samples were extracted with acetonitrile and ammonium acetate buffer and purified by liquid extraction with dichloromethane, and then on MCAX solid-phase extraction cartridges. Then the extract was evaporated at 45°C by nitrogen blow. The residue was dissolved and separated by an Acquity BEH C18 column. The mobile phase was acetonitrile (A) and 5 mmol/L of ammonium acetate containing 0.1% formic acid (B). Analytes were confirmed and quantified using a tandem mass spectrometry system in multiple reaction mode with triple quadrupole analyzer using positive polarity mode. The limits of detection of malachite green, leucomalachite green, crystal violet and leucocrystal violet were 0.15 µg/kg, the limits of quantification were 0.50 µg/kg, and the average recoveries were more than 75% with spiked residues from 0.5 to 10 µg/kg. The relative standard deviations were less than 13%. The limits of detection of methylene blue, azure A, azure B and azure C were 0.3 µg/kg, the limits of quantification were 1.0 µg/kg, the average recoveries were more than 70% with spiked residues from 1.0 to 10 µg/kg and the relative standard deviations were less than 15%. The method has the merits of simplicity, sensitivity and rapidity, and can be used for simultaneous determination of the analytes in aquatic products.

摘要

本研究建立了固相萃取 - 超高效液相色谱 - 电喷雾电离串联质谱法,用于测定水产品中孔雀石绿及其代谢物隐色孔雀石绿、结晶紫及其代谢物隐色结晶紫、亚甲基蓝及其代谢物包括天青A、天青B和天青C。样品用乙腈和醋酸铵缓冲液萃取,经二氯甲烷液液萃取纯化,再通过MC AX固相萃取柱净化。然后将萃取液在45℃下用氮气吹干。残留物用Acquity BEH C18柱溶解并分离。流动相为乙腈(A)和含0.1%甲酸的5 mmol/L醋酸铵(B)。使用具有三重四极杆分析仪的串联质谱系统,在正离子模式下的多反应监测模式下对分析物进行确证和定量。孔雀石绿、隐色孔雀石绿、结晶紫和隐色结晶紫的检出限为0.15 μg/kg,定量限为0.50 μg/kg,在0.5至10 μg/kg加标残留量下平均回收率大于75%,相对标准偏差小于13%。亚甲基蓝、天青A、天青B和天青C的检出限为0.3 μg/kg,定量限为1.0 μg/kg,在1.0至10 μg/kg加标残留量下平均回收率大于70%,相对标准偏差小于15%。该方法具有简便、灵敏、快速的优点,可用于同时测定水产品中的分析物。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验